Abbott Laboratories, Inc recalls

28 recalls on record · latest: February 3, 2022

Official U.S. recall history for Abbott Laboratories, Inc, compiled from official government records.

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Abbott Laboratories, Inc recalls Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)00380740138479 The Alinity s System is intended…

February 3, 2022 · Medical device recalls Moderate risk Software error associated with the immunoassay analyzer wash cycle which is usi…

Abbott Laboratories, Inc recalls Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in blood donor screening,…

July 12, 2021 · Medical device recalls Moderate risk A design defect (hardware and software) allows liquid waste pressure to build u…

Abbott Laboratories, Inc recalls ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated chem…

May 1, 2019 · Medical device recalls Moderate risk Mixer blade may separate from mixer due to the screw and nut failure and detach…

Abbott Laboratories, Inc recalls ARCHITECT MAGNESIUM, (a) REF 7D70-21, (b) 7D70-31 The Magnesium assay is used for the quantitation of magnesium in huma…

January 2, 2019 · Medical device recalls Moderate risk Abbott internal testing has identified that the Magnesium urine application dem…

Abbott Laboratories, Inc recalls APS Accelerator modular systems, 208-230 V-, 50/60 Hz, 1800 VA, IVD, RX, Class 2 Laser Product,

September 7, 2018 · Medical device recalls Moderate risk The firm identified customer sites where modules which the safety pacemaker lab…

Abbott Laboratories, Inc recalls Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHITECT cSystems ICT (Integrated Chip Technolo…

August 28, 2018 · Medical device recalls Moderate risk There is a potential to generate falsely elevated serum or plasma chloride resu…

Abbott Laboratories, Inc recalls Abbott ARCHITECT Creatine Kinase, IVD, REF 7D6341.

July 18, 2018 · Medical device recalls Moderate risk The product has a stability issue which may lead to an error code indicating "U…

Abbott Laboratories, Inc recalls Abbott ARCHITECT Creatine Kinase, IVD, REF 7D63-21.

July 18, 2018 · Medical device recalls Moderate risk The product has a stability issue which may lead to an error code indicating "U…

Abbott Laboratories, Inc recalls Abbott ARCHITECT c4000 Processing Module, List No. 02P24 - Product Usage: The Abbott ARCHITECT System is intended for I…

July 17, 2018 · Medical device recalls Moderate risk There is a potential to generate incorrect results on the instrument if particu…

Abbott Laboratories, Inc recalls Abbott ARCHITECT c16000 Processing Module, List No. 03L77 - Product Usage: The Abbott ARCHITECT System is intended for…

July 17, 2018 · Medical device recalls Moderate risk There is a potential to generate incorrect results on the instrument if particu…

Abbott Laboratories, Inc recalls Abbott ARCHITECT c8000 Processing Module, List No. 01G06 - Product Usage: The Abbott ARCHITECT System is intended for I…

July 17, 2018 · Medical device recalls Moderate risk There is a potential to generate incorrect results on the instrument if particu…

Abbott Laboratories, Inc. recalls CardioMEMS HF System Hospital and Patient Electronics Units: (a) Patient Electronics System, Model CM1100 (b) Hospital…

June 14, 2018 · Medical device recalls Moderate risk Abbott is advising customers that a small number of CardioMEMS(R) Hospital Elec…

Abbott Laboratories, Inc recalls C4 is an in vitro diagnostic assay for the quantitative determination of C4 in human serum or plasma. Antigen in the sa…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls Immunoglobulin M is an in vitro diagnostic assay for the quantitative determination of immunoglobulin M in human serum…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls Apolipoprotein A1 is an in vitro diagnostic assay for the quantitative determination of apolipoprotein A1 in human seru…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls Immunoglobulin A is an in vitro diagnostic assay for the quantitative determination of immunoglobulin A in human serum…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls Immunoglobulin G is an in vitro diagnostic assay for the quantitative determination of immunoglobulin G in human serum…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls Apolipoprotein B is an in vitro diagnostic assay for the quantitative determination of apolipoprotein B in human serum…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls Transferrin is an in vitro diagnostic assay for the quantitative determination of transferrin in human serum or plasma.…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls C3 is an in vitro diagnostic assay for the quantitative determination of C3 in human serum or plasma. Antibodies to C3…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls The,K -ASSAY HP assay is intended for the quantitative determination of human haptoglobin by immunoturbidimetric assay.…

May 16, 2018 · Medical device recalls Moderate risk An update to the Reagents and Specimen Collection and Handling/Preparation for…

Abbott Laboratories, Inc recalls ARCHITECT c8000 Cuvette Segment, Part #01G46-01/01G06, a component to the ARCHITECT Clinical Chemistry system. There ar…

December 8, 2017 · Medical device recalls Moderate risk There is a potential to generate falsely depressed patient results in the cuvet…

Abbott Laboratories, Inc recalls ARCHITECT c4000 Cuvette Segment, Part #02P75-01/02P24, a component to the ARCHITECT Clinical Chemistry system. There ar…

December 8, 2017 · Medical device recalls Moderate risk There is a potential to generate falsely depressed patient results in the cuvet…

Abbott Laboratories, Inc recalls ARCHITECT c16000 Cuvette Segment, Part #09D32-05/ 03L77, a component to the ARCHITECT Clinical Chemistry system. There…

December 8, 2017 · Medical device recalls Moderate risk There is a potential to generate falsely depressed patient results in the cuvet…

Abbott Laboratories, Inc recalls ARCHITECT c4000 part number 02P24; ARCHITECT c8000 part number 01G06; ARCHITECT c16000 part number 03L77 Clinical Chemi…

September 29, 2017 · Medical device recalls Moderate risk The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 ha…

Abbott Laboratories, Inc recalls Tubing, Peristaltic Head Part Number 7-35009685-01 for use in clinical chemistry systems.

September 29, 2017 · Medical device recalls Moderate risk The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 ha…

Abbott Laboratories, Inc recalls ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for In Vitro diagnostic use only. The ARCHITECT system…

September 9, 2015 · Medical device recalls Moderate risk Incorrect tubing.

Abbott Laboratories, Inc recalls ARCHITECT c4000 Cuvette Segment, List number 02P75-01. The firm name on the label is Abbott Laboratories, Abbott Park,…

January 15, 2015 · Medical device recalls Moderate risk There is a potential to generate falsely-depressed patient results in the cuvet…